Taking AIM at Breast Cancer

Breast Cancer Clinical Trial

Official title:

Taking AIM at Breast Cancer: Targeting Adiposity and Inflammation With Movement to Improve Prognosis in Breast Cancer Survivors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04720209
• Other study ID #: 20-172
• Status: Recruiting
• Phase: N/A
• Start date: August 13, 2021
• Est. completion date: June 15, 2026

Study information

• Verified date: January 2024
• Source: Dana-Farber Cancer Institute
• Contact: Christina M Dieli-Conwright, PhD
• Phone: (617) 582-8321
• Email: ChristinaM_Dieli-Conwright[@]dfci.harvard.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this research is to determine whether a 16-week exercise program for individuals with breast cancer and have completed treatment (i.e., surgery, chemotherapy, or radiation) for breast cancer will decrease inflammation in fat tissue.

Description:

This study is about using different types of exercise to reduce inflammation in fat tissue in an effort to minimize the risk of cancer recurrence related to being overweight or obese. The investigators hope to learn whether participating in a specific exercise program can cause inflammation in the fat tissue to decrease.

The names of the study interventions involved in this study are:

• Circuit-style aerobic and resistance exercise (CARE)

• Traditional aerobic and resistance exercise (TARE)

The research study procedures include screening for eligibility, and study treatment including evaluations and follow up visits.

The study treatment will be for 4 months and participants will followed for 8 months.

The total time for participation in this study will be about 12 months. It is expected that about 300 people will take part in this research study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: June 15, 2026
• Est. primary completion date: June 15, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Women diagnosed with breast cancer (all stages excluding stage IV), low grade disease positive for estrogen and progesterone receptors

• Over the age of 18 years; children under the age of 18 will be excluded due to rarity of disease

• The effects of exercise on the developing fetus are unknown. For this reason, women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for six months following duration of study participation. Should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately. Patients must undergo a pregnancy test via urine strip that will be covered and provided by the PI. Urine strips will be utilized over bloodwork for cost effectiveness. Urine tests will be distributed once before DEXA scans.

• Are centrally obese with the following criteria[57] (determined by study team at eligibility screening): BMI >30 kg/m2 (calculated using height and weight; an upper limit BMI will not be set; we will rely on obtaining physicians' clearance to assess full eligibility) or body fat >30% (estimated by bioelectrical impedance), and waist circumference >35 in.

• Have undergone a lumpectomy or mastectomy.

• If cancer treatment included neoadjuvant or adjuvant chemotherapy and/or radiation therapy, participant must have received and completed treatment.

• Speak English

• Is in breast cancer remission with no detectable disease present

• Able to initiate a supervised exercise program (free from any cardiovascular, respiratory or musculoskeletal disease or joint problems that preclude moderate physical activity)

• Free from history of chronic disease including uncontrolled diabetes, hypertension or thyroid disease.

• Have not experienced a weight reduction =10% within the past 6 months

• Currently participate in less than 60 minutes of structured exercise/week

• No planned reconstructive surgery with flap repair during trial and follow-up period

• May use adjuvant endocrine therapy, trastuzumab or pertuzumab if use will be continued for duration of study intervention

• Does not smoke (no smoking during previous 12 months)

• Willing to travel to Dana-Farber Cancer Institute

• Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Patients should not have any uncontrolled illness including ongoing or active infection, uncontrolled diabetes, hypertension or thyroid disease

• Patients may not be receiving any other investigational agents, or concurrent biological, chemotherapy, or radiation therapy

• Patients with other active malignancies are ineligible for this study.

• Patients with metastatic disease

• Is not centrally obese as defined above

• Has not completed surgery, chemotherapy, or radiation treatment associated with their diagnosis

• History of any musculoskeletal, cardiorespiratory or neurological diseases that preclude the participation in exercise

• Participates in more than 60 minutes of structured exercise/week

• Is planning reconstructive surgery with flap repair during trial and follow-up period

• Currently smokes

• Is unable to travel to the exercise facilities

• Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study

Related Conditions & MeSH terms

• Breast Cancer
• Breast Cancer Stage I
• Breast Cancer Stage II
• Breast Cancer Stage III
• Breast Neoplasms

Intervention

Other:
• CARE
CARE is a 16-week, supervised, periodized AE and RE program performed in a circuit fashion 3 days/week on-site
• TARE
TARE is a 16- week, supervised AE and RE program consisting of three sessions per week on-site
• Home-Based Stretching
This group will perform a home-based program of the same stretches utilized in the CARE and TARE groups.

Locations

Country	Name	City	State
United States	Brigham and Women's Hospital	Boston	Massachusetts
United States	Dana Farber Cancer Institute	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Dana-Farber Cancer Institute	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Decrease in adipose tissue levels of inflammation.	Adipose tissue inflammation will be assessed by measuring: M1 and M2 adipose tissue macrophages (ATMs)	16 Weeks
Primary	Decrease in adipose tissue levels of inflammation.	Adipose tissue inflammation will be assessed by measuring: leptin, adiponectin, IL-6 and IL-8	16 weeks
Primary	Decrease in adipose tissue levels of inflammation.	Adipose tissue inflammation will be assessed by measuring: hs-CRP and TNF-a	16 weeks
Secondary	4-month CARE intervention on sarcopenic obesity.	sarcopenic obesity will be assessed via dual energy X-ray absorptiometry using a validated equation.	16 Weeks